Canonical Allele Identifier: CA1955123934
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17397006C= , CM000673.2:g.17397006C= GRCh38
NC_000011.9:g.17418553C= , CM000673.1:g.17418553C= GRCh37
NC_000011.8:g.17375129C= NCBI36
NG_008867.1:g.84897G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3630G=
ENST00000528374.2:c.620G=
ENST00000529967.6:n.2368G=
ENST00000532220.2:n.2277G=
ENST00000642611.2:n.4244G=
ENST00000644057.2:n.472G=
ENST00000645004.2:n.1528G=
ENST00000682051.1:n.4191G=
ENST00000682110.1:n.4244G=
ENST00000682140.1:c.3985+187G= ENSP00000507829.1:n.3985+187G=
ENST00000682185.1:n.5334G=
ENST00000682204.1:c.*2167G= ENSP00000507094.1:n.*2167G=
ENST00000682215.1:n.4611G=
ENST00000682288.1:c.*2460G= ENSP00000507506.1:n.*2460G=
ENST00000682442.1:n.4464G=
ENST00000682528.1:n.4321G=
ENST00000682673.1:n.4188G=
ENST00000682805.1:n.4611G=
ENST00000682965.1:c.*451G= ENSP00000508229.1:n.*451G=
ENST00000683093.1:n.4343G=
ENST00000683136.1:c.3912G= ENSP00000507768.1:p.Lys1304=
ENST00000683153.1:n.4286G=
ENST00000683365.1:n.4346G=
ENST00000683377.1:n.4244G=
ENST00000683456.1:c.*1166G= ENSP00000508318.1:n.*1166G=
ENST00000683522.1:n.4244G=
ENST00000683562.1:c.*2198G= ENSP00000508265.1:n.*2198G=
ENST00000683693.1:n.4691G=
ENST00000683725.1:c.4029G= ENSP00000507496.1:p.Lys1343=
ENST00000684010.1:n.4239G=
ENST00000684157.1:n.4244G=
ENST00000684253.1:n.4147G=
ENST00000684288.1:c.*2201G= ENSP00000507143.1:n.*2201G=
ENST00000684313.1:n.3676G=
ENST00000684332.1:n.4317G=
ENST00000684371.1:n.4350G=
ENST00000684404.1:n.4287G=
ENST00000684442.1:n.4468G=
ENST00000684555.1:c.*2241G= ENSP00000507705.1:n.*2241G=
ENST00000684571.1:c.3870G= ENSP00000506935.1:p.Lys1290=
ENST00000684593.1:c.*3734G= ENSP00000507005.1:n.*3734G=
ENST00000684711.1:c.*2425G= ENSP00000506841.1:n.*2425G=
ENST00000302539.9:c.4032G= ENSP00000303960.4:p.Lys1344=
ENST00000389817.8:c.4029G= MANE Select ENSP00000374467.4:p.Lys1343=
ENST00000642271.1:c.4026G= ENSP00000493749.1:p.Lys1342=
ENST00000642579.1:c.2083G=
ENST00000642611.1:n.4129G=
ENST00000642902.1:c.3811G=
ENST00000643260.1:c.4029G= ENSP00000494450.1:p.Lys1343=
ENST00000643562.1:c.*2151G= ENSP00000496124.1:n.*2151G=
ENST00000643925.1:c.2669G=
ENST00000644057.1:n.106G=
ENST00000644484.1:c.*2430G= ENSP00000493558.1:n.*2430G=
ENST00000644675.1:c.*2201G= ENSP00000494567.1:n.*2201G=
ENST00000644757.1:c.*2460G= ENSP00000495085.1:n.*2460G=
ENST00000644772.1:c.4095G= ENSP00000494321.1:p.Lys1365=
ENST00000645004.1:n.1684G=
ENST00000645076.1:c.3228G=
ENST00000645417.1:c.1217G=
ENST00000645744.1:c.*2809G= ENSP00000494564.1:n.*2809G=
ENST00000645760.1:c.4450G=
ENST00000645884.1:c.*1312G= ENSP00000495516.1:n.*1312G=
ENST00000646003.1:c.*2131G= ENSP00000495259.1:n.*2131G=
ENST00000646207.1:c.*2866G= ENSP00000495025.1:n.*2866G=
ENST00000646276.1:c.*2448G= ENSP00000496070.1:n.*2448G=
ENST00000646592.1:c.3335G=
ENST00000646902.1:c.3996G= ENSP00000494101.1:p.Lys1332=
ENST00000646993.1:c.*2571G= ENSP00000493720.1:n.*2571G=
ENST00000647013.1:c.4035G= ENSP00000496741.1:n.4035G=
ENST00000647015.1:c.3780G= ENSP00000495389.1:p.Lys1260=
ENST00000647086.1:c.*3615G= ENSP00000493677.1:n.*3615G=
ENST00000647158.1:c.*2316G= ENSP00000495744.1:n.*2316G=
ENST00000302539.8:c.4032G= ENSP00000303960.4:p.Lys1344=
ENST00000389817.7:c.4029G= ENSP00000374467.3:p.Lys1343=
ENST00000527905.5:c.*1051G= ENSP00000431653.1:n.*1051G=
ENST00000528374.1:c.511G=
ENST00000531137.1:n.594G=
ENST00000531891.1:c.367G=
ENST00000532220.1:n.503G=
NM_000352.4:c.4029G= NP_000343.2:p.Lys1343=
NM_001287174.1:c.4032G= NP_001274103.1:p.Lys1344=
XM_011520331.1:c.4029G= XP_011518633.1:p.Lys1343=
XM_011520332.1:c.4032G= XP_011518634.1:p.Lys1344=
XM_011520333.1:c.2529G= XP_011518635.1:p.Lys843=
XR_930890.1:n.4095G=
NM_001351295.1:c.4095G= NP_001338224.1:p.Lys1365=
NM_001351296.1:c.4029G= NP_001338225.1:p.Lys1343=
NM_001351297.1:c.4026G= NP_001338226.1:p.Lys1342=
NR_147094.1:n.4324G=
XM_017018197.2:c.4098G= XP_016873686.1:p.Lys1366=
XM_017018199.1:c.4095G= XP_016873688.1:p.Lys1365=
XM_017018201.2:c.4098G= XP_016873690.1:p.Lys1366=
XM_017018202.1:c.2595G= XP_016873691.1:p.Lys865=
XM_017018204.1:c.1986G= XP_016873693.1:p.Lys662=
XM_024448668.1:c.2397G= XP_024304436.1:p.Lys799=
XR_001747945.2:n.4170G=
XR_001747946.2:n.4101G=
XR_002957189.1:n.4766G=
NM_000352.6:c.4029G= MANE Select NP_000343.2:p.Lys1343=
NM_001287174.2:c.4032G= NP_001274103.1:p.Lys1344=
NM_001351295.2:c.4095G= NP_001338224.1:p.Lys1365=
NM_001351296.2:c.4029G= NP_001338225.1:p.Lys1343=
NM_001351297.2:c.4026G= NP_001338226.1:p.Lys1342=
NR_147094.2:n.4324G=
NM_001287174.3:c.4032G= NP_001274103.1:p.Lys1344=